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[ Bron: smalt  ]

Pakket: smalt (0.7.6-13)

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Sequence Mapping and Alignment Tool

SMALT efficiently aligns DNA sequencing reads with a reference genome. Reads from a wide range of sequencing platforms, for example Illumina, Roche-454, Ion Torrent, PacBio or ABI-Sanger, can be processed including paired reads.

The software employs a perfect hash index of short words (< 20 nucleotides long), sampled at equidistant steps along the genomic reference sequences.

For each read, potentially matching segments in the reference are identified from seed matches in the index and subsequently aligned with the read using a banded Smith-Waterman algorithm.

The best gapped alignments of each read is reported including a score for the reliability of the best mapping. The user can adjust the trade-off between sensitivity and speed by tuning the length and spacing of the hashed words.

A mode for the detection of split (chimeric) reads is provided. Multi-threaded program execution is supported.

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smalt downloaden

Pakket downloaden voor alle beschikbare platforms
Platform Pakketgrootte Geïnstalleerde grootte Bestanden
alpha (unofficial port) 107,4 kB342,0 kB [overzicht]
amd64 112,1 kB306,0 kB [overzicht]
arm64 102,1 kB342,0 kB [overzicht]
armel 97,2 kB272,0 kB [overzicht]
armhf 95,9 kB200,0 kB [overzicht]
hppa (unofficial port) 110,0 kB298,0 kB [overzicht]
i386 124,1 kB344,0 kB [overzicht]
ia64 (unofficial port) 143,4 kB547,0 kB [overzicht]
m68k (unofficial port) 96,0 kB268,0 kB [overzicht]
mips64el 106,4 kB362,0 kB [overzicht]
ppc64 (unofficial port) 122,6 kB534,0 kB [overzicht]
ppc64el 123,2 kB406,0 kB [overzicht]
riscv64 112,6 kB250,0 kB [overzicht]
s390x 113,7 kB326,0 kB [overzicht]
sh4 (unofficial port) 119,7 kB276,0 kB [overzicht]
sparc64 (unofficial port) 91,4 kB2.073,0 kB [overzicht]
x32 (unofficial port) 111,7 kB296,0 kB [overzicht]